Search research articles
Contact Us
Filters
Showing results (71-80 of 88) with videos related to
Page
of 9
Sort By:
The New England Journal of Medicine
|
October 7, 2020
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, et al.
Nature Cardiovascular Research
|
December 30, 2025
A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects
Irfan S Kathiriya, Martin H Dominguez, Kavitha S Rao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
A novel splice site variant in <i>DEGS1</i> leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved
Holly C Beale, Victor Tse, Joanna Y Lee, et al.
Human Genetics
|
May 6, 2026
A novel splice site variant in DEGS1 leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved
Holly C Beale, Victor Tse, Joanna Y Lee, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
July 19, 2024
Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer: A Phase II Multicenter Study
Collin M Blakely, Anatoly Urisman, Matthew A Gubens, et al.
Clinical Genetics
|
June 6, 2026
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients
Camille Bergès, Clément Sauvestre, Sophie Naudion, et al.
Journal of Neuropathology and Experimental Neurology
|
June 15, 2022
Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma
Calixto-Hope G Lucas, Christian J Davidson, Mouied Alashari, et al.
Developmental Cell
|
December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease
Irfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
NPJ Genomic Medicine
|
May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
Anne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain Pathology (Zurich, Switzerland)
|
October 15, 2019
Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic features
Calixto-Hope G Lucas, Javier E Villanueva-Meyer, Nicholas Whipple, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 88) with videos related to
Sort By:
Page
of 9
The New England Journal of Medicine
|
October 7, 2020
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, et al.
Nature Cardiovascular Research
|
December 30, 2025
A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects
Irfan S Kathiriya, Martin H Dominguez, Kavitha S Rao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
A novel splice site variant in <i>DEGS1</i> leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved
Holly C Beale, Victor Tse, Joanna Y Lee, et al.
Human Genetics
|
May 6, 2026
A novel splice site variant in DEGS1 leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved
Holly C Beale, Victor Tse, Joanna Y Lee, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
July 19, 2024
Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer: A Phase II Multicenter Study
Collin M Blakely, Anatoly Urisman, Matthew A Gubens, et al.
Clinical Genetics
|
June 6, 2026
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients
Camille Bergès, Clément Sauvestre, Sophie Naudion, et al.
Journal of Neuropathology and Experimental Neurology
|
June 15, 2022
Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma
Calixto-Hope G Lucas, Christian J Davidson, Mouied Alashari, et al.
Developmental Cell
|
December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease
Irfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
NPJ Genomic Medicine
|
May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
Anne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Brain Pathology (Zurich, Switzerland)
|
October 15, 2019
Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic features
Calixto-Hope G Lucas, Javier E Villanueva-Meyer, Nicholas Whipple, et al.
Page
of 9